Product Recalls in North Carolina

Product recalls affecting North Carolina — including food, drugs, consumer products, medical devices, and vehicles distributed to North Carolina. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,744 recalls have been distributed to North Carolina in the last 12 months.

54,363 total recalls
1,744 in last 12 months

Showing 5026150280 of 54,363 recalls

Medical DeviceMay 23, 2013· Prism Medical Services USA

Recalled Item: BC Hammock Mesh Sling (Medium) Recalled by Prism Medical Services USA Due to...

The Issue: The product does not meet the firm's size standards, the product was...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2013· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker Instruments 0400-830-000 T4 Toga Recalled by Stryker Instruments...

The Issue: Based on an accelerated aging test for this product packaging, there is an...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
FoodMay 23, 2013· Mother Earth International LLC

Recalled Item: Mother Earth Products Recalled by Mother Earth International LLC Due to...

The Issue: The product was manufactured with a Soy Protein Isolate manufactured by CHS,...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 22, 2013· Elekta, Inc.

Recalled Item: Monaco RTP System Radiation Therapy Treatment Planning System. Radiation...

The Issue: Patient needs to be positioned as indicated by the treatment plan.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2013· Baxter Healthcare Corp.

Recalled Item: Baxter Recalled by Baxter Healthcare Corp. Due to leaking pouches

The Issue: leaking pouches

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
FoodMay 21, 2013· Jus Made, Inc

Recalled Item: Roo's Juice Tropical Orange Flavor (5% juice beverage) 10 FL Recalled by Jus...

The Issue: The product has the potential to contain polysaccharide-based bacterial...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
DrugMay 21, 2013· American Health Packaging

Recalled Item: Zolpidem Tartrate Tablets 5 mg Recalled by American Health Packaging Due to...

The Issue: Unit Dose Mispackaging: This recall event is due to a random undetected...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMay 21, 2013· Baxter Healthcare Corp.

Recalled Item: Heparin Sodium and 0.9% Sodium Chloride Injection Recalled by Baxter...

The Issue: Lack of Assurance of Sterility: Specific lot numbers of these products have...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMay 21, 2013· Baxter Healthcare Corp.

Recalled Item: 0.9% Sodium Chloride Injection Recalled by Baxter Healthcare Corp. Due to...

The Issue: Lack of Assurance of Sterility: Specific lot numbers of these products have...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMay 21, 2013· Fresenius Kabi USA, LLC

Recalled Item: Folic Acid Injection Recalled by Fresenius Kabi USA, LLC Due to Failed...

The Issue: Failed Impurities/Degradation Specification

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugMay 21, 2013· Sun Pharmaceutical Industries Inc.

Recalled Item: Nimodipine Capsules 30 mg Recalled by Sun Pharmaceutical Industries Inc. Due...

The Issue: Crystallization; crystallized nimodipine

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMay 21, 2013· Baxter Healthcare Corp.

Recalled Item: Sodium Chloride Injection Recalled by Baxter Healthcare Corp. Due to Lack of...

The Issue: Lack of Assurance of Sterility: Specific lot numbers of these products have...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMay 21, 2013· Baxter Healthcare Corp.

Recalled Item: Lidocaine Hydrochloride and 5% Dextrose Injection Recalled by Baxter...

The Issue: Lack of Assurance of Sterilty: Specific lot numbers of these products have...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMay 21, 2013· Baxter Healthcare Corp.

Recalled Item: 5% Dextrose Injection Recalled by Baxter Healthcare Corp. Due to Lack of...

The Issue: Lack of Assurance of Sterility: Specific lot numbers of these products have...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMay 21, 2013· Baxter Healthcare Corp.

Recalled Item: Metronidazole Injection USP Recalled by Baxter Healthcare Corp. Due to Lack...

The Issue: Lack of Assurance of Sterility: Specific lot numbers of these products have...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMay 20, 2013· Hospira, Inc.

Recalled Item: Ondansetron Injection Recalled by Hospira, Inc. Due to Presence of...

The Issue: Presence of Particulate; lot being recalled as a precaution due to the...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMay 20, 2013· Sandoz Incorporated

Recalled Item: Methotrexate Injection Recalled by Sandoz Incorporated Due to Presence of...

The Issue: Presence of Particulate Matter: Found during examination of retention samples.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugMay 20, 2013· Dolphin Intertrade Corporation

Recalled Item: JaDera Recalled by Dolphin Intertrade Corporation Due to Undeclared Sibutramine

The Issue: Marketed without an Approved NDA/ANDA: Products found to contain undeclared...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugMay 20, 2013· Dolphin Intertrade Corporation

Recalled Item: XIYOUJI QINGZHI CAPSULE Recalled by Dolphin Intertrade Corporation Due to...

The Issue: Marketed without an Approved NDA/ANDA: Products found to contain undeclared...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 20, 2013· Steris Corporation

Recalled Item: STERIS Fine Traction Device Recalled by Steris Corporation Due to A bearing...

The Issue: A bearing used in the assembly of the Fine Traction Device did not perform...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing